Review



target-specific sirnas  (Santa Cruz Biotechnology)


Bioz Verified Symbol Santa Cruz Biotechnology is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Santa Cruz Biotechnology target-specific sirnas
    Target Specific Sirnas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/target+specific+sirnas/pm40499874-76-5-25
    Average 90 stars, based on 1 article reviews
    target-specific sirnas - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Knockdown:

    Article Title: Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC-associated factor X.
    Article Snippet: Nan Qin, Aguirre A. de Cubas, Ruben Garcia-Martin, Susan Richter, Mirko Peitzsch, Mario Menschikowski, Jacques W.M.. Lenders, Henri J. L. M. Timmers, Massimo Mannelli, Giuseppe Opocher, Matina Economopoulou, Gabriele Siegert, Triantafyllos Chavakis, Karel Pacak, Mercedes Robledo and Graeme Eisenhofer 1 Institute of Clinical Chemistry and Laboratory Medicine, Technische Universit€at Dresden, Dresden, Germany 2 Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain 3 Department of Clinical Pathobiochemistry, Technische Universit€at Dresden, Dresden, Germany 4 Medical Clinic III, Technische Universit€at Dresden, Dresden, Germany 5 Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands 6 Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy 7 Familial Cancer Clinic and Oncoendocrinology, Veneto Institute of Oncology IRCCS, Padova, Italy 8 Department of Medicine, University of Padova, Padova, Italy 9 Department of Ophthalmology, Technische Universit€at Dresden, Dresden, Germany 10 Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Washington DC, Bethesda, MD

    Article Title: Human Schlafen 5 (SLFN5) Is a Regulator of Motility and Invasiveness of Renal Cell Carcinoma Cells
    Article Snippet: 116 117 7 RNAi knockdown of SLFN5 118 Transient knockdown of SLFN5, MMP-1 and MMP-13 was performed using a pool of 119 three target-specific siRNAs as well as non-targeting control pool siRNA, purchased 120 from Santa Cruz Biotechnology, using Lipofectamine RNAiMAX (Invitrogen) as per the 121 manufacturer’s instructions.

    Article Title: The siRNA-mediated downregulation of N-Ras sensitizes human melanoma cells to apoptosis induced by selective BRAF inhibitors.
    Article Snippet: The clinical benefit of selective BRAF inhibitor therapies is limited by the emergence of drug resistance.. Here, we investigated the molecular basis underlying the acquired resistance to a BRAF inhibitor by comparing the signaling pathways in the parental A375P cells and the resistant subline (A375P/Mdr).. We demonstrate that MAPK re-activation does not contribute to the mechanism of resistance to UAI-201 of A375P/Mdr cells.

    Article Title: Down-regulation of c-Cbl by Morphine Accounts for Persistent ERK1/2 Signaling in δ-Opioid Receptor-expressing HEK293 Cells
    Article Snippet: Knockdown of c-Cbl expression was achieved by transfection of HEK/DOR cells with three target-specific siRNAs (Santa Cruz Biotechnology, Santa Cruz, CA) according to themanufacturer’s protocol.

    Article Title: Differential regulation of PTEN expression by androgen receptor in prostate and breast cancers.
    Article Snippet: Control siRNA was a pool of four-scrambled non-specific siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA).

    Article Title: Apoptosis linked gene-2 interacting protein X as a target to regulate the yield of small extracellular vesicles derived from tissue specific mesenchymal stem cells for translational applications.
    Article Snippet: Small extracellular vesicles (sEVs) derived from mesenchymal stem cells (MSCs) have emerged as promising therapeutic agents in regenerative medicine.. However, their clinical translation remains limited by low production yields.. The prime objective of this study was aimed at dissecting the regulatory mechanisms of sEV biogenesis in MSCs by investigating the roles of key proteins involved in both ESCRT-dependent (HRS, STAM, TSG101, ALIX) and ESCRT-independent (RAB27A, RAB27B) pathways.

    Control:

    Article Title: Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC-associated factor X.
    Article Snippet: Nan Qin, Aguirre A. de Cubas, Ruben Garcia-Martin, Susan Richter, Mirko Peitzsch, Mario Menschikowski, Jacques W.M.. Lenders, Henri J. L. M. Timmers, Massimo Mannelli, Giuseppe Opocher, Matina Economopoulou, Gabriele Siegert, Triantafyllos Chavakis, Karel Pacak, Mercedes Robledo and Graeme Eisenhofer 1 Institute of Clinical Chemistry and Laboratory Medicine, Technische Universit€at Dresden, Dresden, Germany 2 Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain 3 Department of Clinical Pathobiochemistry, Technische Universit€at Dresden, Dresden, Germany 4 Medical Clinic III, Technische Universit€at Dresden, Dresden, Germany 5 Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands 6 Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy 7 Familial Cancer Clinic and Oncoendocrinology, Veneto Institute of Oncology IRCCS, Padova, Italy 8 Department of Medicine, University of Padova, Padova, Italy 9 Department of Ophthalmology, Technische Universit€at Dresden, Dresden, Germany 10 Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Washington DC, Bethesda, MD

    Article Title: Human Schlafen 5 (SLFN5) Is a Regulator of Motility and Invasiveness of Renal Cell Carcinoma Cells
    Article Snippet: 116 117 7 RNAi knockdown of SLFN5 118 Transient knockdown of SLFN5, MMP-1 and MMP-13 was performed using a pool of 119 three target-specific siRNAs as well as non-targeting control pool siRNA, purchased 120 from Santa Cruz Biotechnology, using Lipofectamine RNAiMAX (Invitrogen) as per the 121 manufacturer’s instructions.

    Article Title: The siRNA-mediated downregulation of N-Ras sensitizes human melanoma cells to apoptosis induced by selective BRAF inhibitors.
    Article Snippet: The clinical benefit of selective BRAF inhibitor therapies is limited by the emergence of drug resistance.. Here, we investigated the molecular basis underlying the acquired resistance to a BRAF inhibitor by comparing the signaling pathways in the parental A375P cells and the resistant subline (A375P/Mdr).. We demonstrate that MAPK re-activation does not contribute to the mechanism of resistance to UAI-201 of A375P/Mdr cells.

    Article Title: Down-regulation of c-Cbl by Morphine Accounts for Persistent ERK1/2 Signaling in δ-Opioid Receptor-expressing HEK293 Cells
    Article Snippet: Knockdown of c-Cbl expression was achieved by transfection of HEK/DOR cells with three target-specific siRNAs (Santa Cruz Biotechnology, Santa Cruz, CA) according to themanufacturer’s protocol.

    Article Title: Differential regulation of PTEN expression by androgen receptor in prostate and breast cancers.
    Article Snippet: Control siRNA was a pool of four-scrambled non-specific siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA).

    Article Title: Apoptosis linked gene-2 interacting protein X as a target to regulate the yield of small extracellular vesicles derived from tissue specific mesenchymal stem cells for translational applications.
    Article Snippet: Small extracellular vesicles (sEVs) derived from mesenchymal stem cells (MSCs) have emerged as promising therapeutic agents in regenerative medicine.. However, their clinical translation remains limited by low production yields.. The prime objective of this study was aimed at dissecting the regulatory mechanisms of sEV biogenesis in MSCs by investigating the roles of key proteins involved in both ESCRT-dependent (HRS, STAM, TSG101, ALIX) and ESCRT-independent (RAB27A, RAB27B) pathways.

    Expressing:

    Article Title: Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC-associated factor X.
    Article Snippet: Nan Qin, Aguirre A. de Cubas, Ruben Garcia-Martin, Susan Richter, Mirko Peitzsch, Mario Menschikowski, Jacques W.M.. Lenders, Henri J. L. M. Timmers, Massimo Mannelli, Giuseppe Opocher, Matina Economopoulou, Gabriele Siegert, Triantafyllos Chavakis, Karel Pacak, Mercedes Robledo and Graeme Eisenhofer 1 Institute of Clinical Chemistry and Laboratory Medicine, Technische Universit€at Dresden, Dresden, Germany 2 Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain 3 Department of Clinical Pathobiochemistry, Technische Universit€at Dresden, Dresden, Germany 4 Medical Clinic III, Technische Universit€at Dresden, Dresden, Germany 5 Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands 6 Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy 7 Familial Cancer Clinic and Oncoendocrinology, Veneto Institute of Oncology IRCCS, Padova, Italy 8 Department of Medicine, University of Padova, Padova, Italy 9 Department of Ophthalmology, Technische Universit€at Dresden, Dresden, Germany 10 Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Washington DC, Bethesda, MD

    Article Title: Human Schlafen 5 (SLFN5) Is a Regulator of Motility and Invasiveness of Renal Cell Carcinoma Cells
    Article Snippet: 116 117 7 RNAi knockdown of SLFN5 118 Transient knockdown of SLFN5, MMP-1 and MMP-13 was performed using a pool of 119 three target-specific siRNAs as well as non-targeting control pool siRNA, purchased 120 from Santa Cruz Biotechnology, using Lipofectamine RNAiMAX (Invitrogen) as per the 121 manufacturer’s instructions.

    Article Title: The siRNA-mediated downregulation of N-Ras sensitizes human melanoma cells to apoptosis induced by selective BRAF inhibitors.
    Article Snippet: The clinical benefit of selective BRAF inhibitor therapies is limited by the emergence of drug resistance.. Here, we investigated the molecular basis underlying the acquired resistance to a BRAF inhibitor by comparing the signaling pathways in the parental A375P cells and the resistant subline (A375P/Mdr).. We demonstrate that MAPK re-activation does not contribute to the mechanism of resistance to UAI-201 of A375P/Mdr cells.

    Article Title: Down-regulation of c-Cbl by Morphine Accounts for Persistent ERK1/2 Signaling in δ-Opioid Receptor-expressing HEK293 Cells
    Article Snippet: Knockdown of c-Cbl expression was achieved by transfection of HEK/DOR cells with three target-specific siRNAs (Santa Cruz Biotechnology, Santa Cruz, CA) according to themanufacturer’s protocol.

    Article Title: Differential regulation of PTEN expression by androgen receptor in prostate and breast cancers.
    Article Snippet: Control siRNA was a pool of four-scrambled non-specific siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA).

    Article Title: Apoptosis linked gene-2 interacting protein X as a target to regulate the yield of small extracellular vesicles derived from tissue specific mesenchymal stem cells for translational applications.
    Article Snippet: Small extracellular vesicles (sEVs) derived from mesenchymal stem cells (MSCs) have emerged as promising therapeutic agents in regenerative medicine.. However, their clinical translation remains limited by low production yields.. The prime objective of this study was aimed at dissecting the regulatory mechanisms of sEV biogenesis in MSCs by investigating the roles of key proteins involved in both ESCRT-dependent (HRS, STAM, TSG101, ALIX) and ESCRT-independent (RAB27A, RAB27B) pathways.

    Transfection:

    Article Title: Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC-associated factor X.
    Article Snippet: Nan Qin, Aguirre A. de Cubas, Ruben Garcia-Martin, Susan Richter, Mirko Peitzsch, Mario Menschikowski, Jacques W.M.. Lenders, Henri J. L. M. Timmers, Massimo Mannelli, Giuseppe Opocher, Matina Economopoulou, Gabriele Siegert, Triantafyllos Chavakis, Karel Pacak, Mercedes Robledo and Graeme Eisenhofer 1 Institute of Clinical Chemistry and Laboratory Medicine, Technische Universit€at Dresden, Dresden, Germany 2 Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and ISCIII Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain 3 Department of Clinical Pathobiochemistry, Technische Universit€at Dresden, Dresden, Germany 4 Medical Clinic III, Technische Universit€at Dresden, Dresden, Germany 5 Internal Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands 6 Department of Experimental and Clinical Biomedical Sciences, University of Florence, Florence, Italy 7 Familial Cancer Clinic and Oncoendocrinology, Veneto Institute of Oncology IRCCS, Padova, Italy 8 Department of Medicine, University of Padova, Padova, Italy 9 Department of Ophthalmology, Technische Universit€at Dresden, Dresden, Germany 10 Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Washington DC, Bethesda, MD

    Article Title: Human Schlafen 5 (SLFN5) Is a Regulator of Motility and Invasiveness of Renal Cell Carcinoma Cells
    Article Snippet: 116 117 7 RNAi knockdown of SLFN5 118 Transient knockdown of SLFN5, MMP-1 and MMP-13 was performed using a pool of 119 three target-specific siRNAs as well as non-targeting control pool siRNA, purchased 120 from Santa Cruz Biotechnology, using Lipofectamine RNAiMAX (Invitrogen) as per the 121 manufacturer’s instructions.

    Article Title: The siRNA-mediated downregulation of N-Ras sensitizes human melanoma cells to apoptosis induced by selective BRAF inhibitors.
    Article Snippet: The clinical benefit of selective BRAF inhibitor therapies is limited by the emergence of drug resistance.. Here, we investigated the molecular basis underlying the acquired resistance to a BRAF inhibitor by comparing the signaling pathways in the parental A375P cells and the resistant subline (A375P/Mdr).. We demonstrate that MAPK re-activation does not contribute to the mechanism of resistance to UAI-201 of A375P/Mdr cells.

    Article Title: Down-regulation of c-Cbl by Morphine Accounts for Persistent ERK1/2 Signaling in δ-Opioid Receptor-expressing HEK293 Cells
    Article Snippet: Knockdown of c-Cbl expression was achieved by transfection of HEK/DOR cells with three target-specific siRNAs (Santa Cruz Biotechnology, Santa Cruz, CA) according to themanufacturer’s protocol.

    Article Title: Differential regulation of PTEN expression by androgen receptor in prostate and breast cancers.
    Article Snippet: Control siRNA was a pool of four-scrambled non-specific siRNA (Santa Cruz Biotechnology, Santa Cruz, CA, USA).

    Article Title: Apoptosis linked gene-2 interacting protein X as a target to regulate the yield of small extracellular vesicles derived from tissue specific mesenchymal stem cells for translational applications.
    Article Snippet: Small extracellular vesicles (sEVs) derived from mesenchymal stem cells (MSCs) have emerged as promising therapeutic agents in regenerative medicine.. However, their clinical translation remains limited by low production yields.. The prime objective of this study was aimed at dissecting the regulatory mechanisms of sEV biogenesis in MSCs by investigating the roles of key proteins involved in both ESCRT-dependent (HRS, STAM, TSG101, ALIX) and ESCRT-independent (RAB27A, RAB27B) pathways.



    Similar Products

    86
    Sangon Biotech target specific tyr sirna sirna tyr
    Target Specific Tyr Sirna Sirna Tyr, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/sequence+specific/pm41605397-98-0-13
    Average 86 stars, based on 1 article reviews
    target specific tyr sirna sirna tyr - by Bioz Stars, 2026-09
    86/100 stars
      Buy from Supplier

    86
    Sangon Biotech gene specific sirna targeting nf1
    A Evolutionary conservation analysis of the mutated residues in CARS1 p.E712V and ( E ) <t>NF1</t> p.Q2002X across species. B , F Domain architecture of CARS1 and NF1. C , G Homology-based three-dimensional structural models of wild-type (WT) and mutant CARS1/NF1 proteins generated using SWISS-MODEL and visualized in PyMOL ( D , H ). Protein-protein interaction networks (STRING database) for CARS1 and NF1.
    Gene Specific Sirna Targeting Nf1, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/sequences+sirna/pmc12855827-335-0-19
    Average 86 stars, based on 1 article reviews
    gene specific sirna targeting nf1 - by Bioz Stars, 2026-09
    86/100 stars
      Buy from Supplier

    94
    OriGene gene specific 27mer sirna duplexes targeting nr4a1
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Gene Specific 27mer Sirna Duplexes Targeting Nr4a1, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/Nr4a1+Rat+siRNA+Oligo+Duplex/pmc13078925-25-0-28
    Average 94 stars, based on 1 article reviews
    gene specific 27mer sirna duplexes targeting nr4a1 - by Bioz Stars, 2026-09
    94/100 stars
      Buy from Supplier

    90
    Ribobio co sirnas on-target and non-specific control
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirnas On Target And Non Specific Control, supplied by Ribobio co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/sirnas+on+target+and+non+specific+control/pmc12271488-51-1-9
    Average 90 stars, based on 1 article reviews
    sirnas on-target and non-specific control - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Shanghai GenePharma sirnas specifically targeting porcine dusp1
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirnas Specifically Targeting Porcine Dusp1, supplied by Shanghai GenePharma, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/pex3+vector/pmc10927503__pnas__2312150121__sapp-167-13-29
    Average 90 stars, based on 1 article reviews
    sirnas specifically targeting porcine dusp1 - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Bioneer Corporation sirnas targeting specific genes
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirnas Targeting Specific Genes, supplied by Bioneer Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/gene+specific+sirna/pm40544760-112-1-8
    Average 90 stars, based on 1 article reviews
    sirnas targeting specific genes - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Shanghai GenePharma sirnas specifically targeting acta2 and vegfa, as well as non-targeting control
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirnas Specifically Targeting Acta2 And Vegfa, As Well As Non Targeting Control, supplied by Shanghai GenePharma, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/primers+of+zo+1++occludin++acta2+and+gapdh/pm40492378-378-9-27
    Average 90 stars, based on 1 article reviews
    sirnas specifically targeting acta2 and vegfa, as well as non-targeting control - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Sangon Biotech sirna specifically targeting c-myc (si-myc)
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirna Specifically Targeting C Myc (Si Myc), supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/sirna+specifically+targeting+c+myc++si+myc+/pm40494182-92-15-23
    Average 90 stars, based on 1 article reviews
    sirna specifically targeting c-myc (si-myc) - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Santa Cruz Biotechnology target-specific sirnas
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Target Specific Sirnas, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/target+specific+sirnas/pm40499874-76-5-25
    Average 90 stars, based on 1 article reviews
    target-specific sirnas - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    90
    Shanghai GenePharma sirnas specific targeting tead1 and a scramble negative control sirna
    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting <t>Nr4a1</t> (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and <t>siNr4a1,</t> 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.
    Sirnas Specific Targeting Tead1 And A Scramble Negative Control Sirna, supplied by Shanghai GenePharma, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/target-specific+sirnas/sirna+targeting+tead1/pmc12177558-72-7-16
    Average 90 stars, based on 1 article reviews
    sirnas specific targeting tead1 and a scramble negative control sirna - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    A Evolutionary conservation analysis of the mutated residues in CARS1 p.E712V and ( E ) NF1 p.Q2002X across species. B , F Domain architecture of CARS1 and NF1. C , G Homology-based three-dimensional structural models of wild-type (WT) and mutant CARS1/NF1 proteins generated using SWISS-MODEL and visualized in PyMOL ( D , H ). Protein-protein interaction networks (STRING database) for CARS1 and NF1.

    Journal: NPJ Genomic Medicine

    Article Title: Identification and validation of CARS1 p.E712V and NF1 p.Q2002X in sporadic Moyamoya disease across 30 trio pedigrees

    doi: 10.1038/s41525-025-00539-8

    Figure Lengend Snippet: A Evolutionary conservation analysis of the mutated residues in CARS1 p.E712V and ( E ) NF1 p.Q2002X across species. B , F Domain architecture of CARS1 and NF1. C , G Homology-based three-dimensional structural models of wild-type (WT) and mutant CARS1/NF1 proteins generated using SWISS-MODEL and visualized in PyMOL ( D , H ). Protein-protein interaction networks (STRING database) for CARS1 and NF1.

    Article Snippet: Gene-specific siRNA targeting NF1, siRNA/overexpression constructs for CARS1, and the CARS1 p.E712V mutant plasmid were custom-designed and generated by Sangon Biotech (Shanghai, China).

    Techniques: Mutagenesis, Generated

    A ~ E results of protein and phenotype experiments of NF1 gene; F ~ K results of protein and phenotype experiments of CARS1 gene. A Representative images of western blotting for NF1 and GAPDH. The statistical results of mRNA and protein expression were calculated. n = 3, ** P < 0.01, **** P < 0.0001. B Representative images of western blotting for VEGF and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3. C Effect of silencing NF1 on the proliferative capacity of HBMEC. n = 3, * P < 0.05, ** P < 0.01, **** P < 0.0001. D The tubule-like structure formation of HBMEC in the NF1-silenced group and the statistical comparison of the number of branch points and total capillary length. n = 3, * P < 0.05, ** P < 0.01. E Effect of silencing NF1 on HBMEC cell migration. n = 3, * P < 0.05. F Representative images of western blotting for CARS1 and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3, *** P < 0.001, **** P < 0.0001. G Effect of different treatments of CARS1 on the relative proliferative capacity of HBMEC. n = 3, **** P < 0.0001. H Representative images of western blotting for GPx4 and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3, * P < 0.05. I Representative images of western blotting for VEGF and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3. J The tubule-like structure formation of HBMEC in the CARS1 treatment group and the statistical comparison of the number of branch points and total capillary length between treatment groups. K Effect of Effect of different treatments of CARS1 on HBMEC cell migration. n = 3, ** P < 0.01, * P < 0.05, **** P < 0.0001. siNF1 NF1 silencing, siCARS1 CARS1 silencing, ev empty vector, CARS1-oe, CARS1 overexpression, CARS1-mut cells expressing the CARS1 p.E712V mutant, nc negative control.

    Journal: NPJ Genomic Medicine

    Article Title: Identification and validation of CARS1 p.E712V and NF1 p.Q2002X in sporadic Moyamoya disease across 30 trio pedigrees

    doi: 10.1038/s41525-025-00539-8

    Figure Lengend Snippet: A ~ E results of protein and phenotype experiments of NF1 gene; F ~ K results of protein and phenotype experiments of CARS1 gene. A Representative images of western blotting for NF1 and GAPDH. The statistical results of mRNA and protein expression were calculated. n = 3, ** P < 0.01, **** P < 0.0001. B Representative images of western blotting for VEGF and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3. C Effect of silencing NF1 on the proliferative capacity of HBMEC. n = 3, * P < 0.05, ** P < 0.01, **** P < 0.0001. D The tubule-like structure formation of HBMEC in the NF1-silenced group and the statistical comparison of the number of branch points and total capillary length. n = 3, * P < 0.05, ** P < 0.01. E Effect of silencing NF1 on HBMEC cell migration. n = 3, * P < 0.05. F Representative images of western blotting for CARS1 and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3, *** P < 0.001, **** P < 0.0001. G Effect of different treatments of CARS1 on the relative proliferative capacity of HBMEC. n = 3, **** P < 0.0001. H Representative images of western blotting for GPx4 and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3, * P < 0.05. I Representative images of western blotting for VEGF and GAPDH. Relative grey values of the protein bands are shown, and the statistical results of protein expression were calculated. n = 3. J The tubule-like structure formation of HBMEC in the CARS1 treatment group and the statistical comparison of the number of branch points and total capillary length between treatment groups. K Effect of Effect of different treatments of CARS1 on HBMEC cell migration. n = 3, ** P < 0.01, * P < 0.05, **** P < 0.0001. siNF1 NF1 silencing, siCARS1 CARS1 silencing, ev empty vector, CARS1-oe, CARS1 overexpression, CARS1-mut cells expressing the CARS1 p.E712V mutant, nc negative control.

    Article Snippet: Gene-specific siRNA targeting NF1, siRNA/overexpression constructs for CARS1, and the CARS1 p.E712V mutant plasmid were custom-designed and generated by Sangon Biotech (Shanghai, China).

    Techniques: Western Blot, Expressing, Comparison, Migration, Plasmid Preparation, Over Expression, Mutagenesis, Negative Control

    Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting Nr4a1 (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and siNr4a1, 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.

    Journal: The Journal of Reproduction and Development

    Article Title: Functional roles of NR4A transcription factors in GnRH regulation of gonadotropin gene expression and secretion in rat primary pituitary cells

    doi: 10.1262/jrd.2025-100

    Figure Lengend Snippet: Effects of Nr4a gene knockdown on gonadotropin gene expression. Primary rat pituitary cells were transfected with siRNAs targeting Nr4a1 (A), Nr4a2 (B), or Nr4a3 (C). Control cells (siCont) were transfected with a non-targeting control siRNA. Gene expression of the gonadotropin subunit was assessed following treatment with or without GnRHa (10 −8 M, three hours). The experiment was repeated at least three times, and representative data are shown. Values are expressed as means ± SEM (n = 4). Statistical significance was determined using the Tukey-Kramer test. * P < 0.05, ** P < 0.01, *** P < 0.001 between siCont and siNr4a1, 2 or 3; ## P < 0.01, ### P < 0.001 vs . Cont.

    Article Snippet: Gene-specific 27mer siRNA duplexes targeting Nr4a1 (siNr4a1, #SR500720B), Nr4a2 (siNr4a2, #SR513154C), and Nr4a3 (siNr4a3, #SR500165A) and a universal scrambled negative control siRNA duplex (siCont, #SR30004) were purchased from OriGene Technologies (Rockville, MD, USA).

    Techniques: Knockdown, Gene Expression, Transfection, Control

    Effects of Nr4a gene knockdown on gonadotropin secretion. Primary cultured rat pituitary cells were transfected with siRNAs targeting Nr4a1 , Nr4a2 , or Nr4a3 (siCont) and with a control siRNA. After incubation with or without GnRHa (10 −8 M, three hours), FSH (A) and LH (B) concentrations in the culture supernatant were measured. The experiment was repeated at least three times, and representative results are presented. Data are shown as means ± SEM (n = 4). Statistical analysis was conducted using the Tukey-Kramer test. *** P < 0.001 between siCont and siNr4a1, 2 or 3; ### P < 0.001 vs . Cont.

    Journal: The Journal of Reproduction and Development

    Article Title: Functional roles of NR4A transcription factors in GnRH regulation of gonadotropin gene expression and secretion in rat primary pituitary cells

    doi: 10.1262/jrd.2025-100

    Figure Lengend Snippet: Effects of Nr4a gene knockdown on gonadotropin secretion. Primary cultured rat pituitary cells were transfected with siRNAs targeting Nr4a1 , Nr4a2 , or Nr4a3 (siCont) and with a control siRNA. After incubation with or without GnRHa (10 −8 M, three hours), FSH (A) and LH (B) concentrations in the culture supernatant were measured. The experiment was repeated at least three times, and representative results are presented. Data are shown as means ± SEM (n = 4). Statistical analysis was conducted using the Tukey-Kramer test. *** P < 0.001 between siCont and siNr4a1, 2 or 3; ### P < 0.001 vs . Cont.

    Article Snippet: Gene-specific 27mer siRNA duplexes targeting Nr4a1 (siNr4a1, #SR500720B), Nr4a2 (siNr4a2, #SR513154C), and Nr4a3 (siNr4a3, #SR500165A) and a universal scrambled negative control siRNA duplex (siCont, #SR30004) were purchased from OriGene Technologies (Rockville, MD, USA).

    Techniques: Knockdown, Cell Culture, Transfection, Control, Incubation